Yeda Research & Development Co. v. Abbott GmbH & Co. KG , 837 F.3d 1341 ( 2016 )


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  •   United States Court of Appeals
    for the Federal Circuit
    ______________________
    YEDA RESEARCH AND DEVELOPMENT CO., LTD.,
    Plaintiff-Appellant
    v.
    ABBOTT GMBH & CO. KG,
    Defendant-Appellee
    ______________________
    2015-1662
    ______________________
    Appeal from the United States District Court for the
    District of Columbia in No. 1:10-cv-01836-RMC, Judge
    Rosemary M. Collyer.
    --------------------------------------------------------------------------
    ABBOTT GMBH & CO. KG,
    Plaintiff-Appellee
    v.
    YEDA RESEARCH AND DEVELOPMENT CO., LTD.,
    Defendant-Appellant
    ______________________
    2015-1663
    ______________________
    2         YEDA RESEARCH AND DEVELOPMENT    v. ABBOTT GMBH
    & CO. KG
    Appeal from the United States District Court for the
    District of Columbia in No. 1:00-cv-01720-RMU, Judge
    Ricardo M. Urbina.
    ______________________
    Decided: September 20, 2016
    ______________________
    MATTHEW NIELSEN, Marshall, Gerstein & Borun LLP,
    Chicago, IL, argued for plaintiff-appellant/defendant-
    appellant. Also represented by KEVIN M. FLOWERS,
    AMANDA ANTONS; ROGER L. BROWDY, RONNI JILLIONS,
    Browdy and Neimark PLLC, Washington, DC.
    JAMES RICHARD FERGUSON, Mayer Brown, LLP, Chi-
    cago, IL, argued for defendant-appellee/plaintiff-appellee.
    Also represented by TODD RAY WALTERS, Buchanan
    Ingersoll & Rooney P.C., Alexandria, VA.
    ______________________
    Before REYNA, WALLACH, and HUGHES, Circuit Judges.
    REYNA, Circuit Judge.
    Yeda Research and Development Co., Ltd. (“Yeda”)
    appeals two decisions by the United States District Court
    for the District of Columbia—one decided in 2008 (No.
    2015-1663) and the other in 2015 (No. 2015-1662). Both
    district court decisions reviewed determinations by the
    Board of Patent Appeals and Interferences regarding
    Yeda’s assertion that Abbott GmbH & Co. KG’s (“Abbott”)
    U.S. Patent No. 5,344,915 (the “’915 patent”) is invalid as
    anticipated.
    The ’915 patent’s invalidity turns on whether it bene-
    fits from the filing dates from either of two German
    patent applications—P39 15 072 (the “’072 application”)
    and P39 22 089 (the “’089 application”). J.A. 5006. If it
    does, then the field of prior art narrows to exclude the
    YEDA RESEARCH AND DEVELOPMENT V. ABBOTT GMBH             3
    & CO. KG
    anticipating reference. Whether the ’915 patent is enti-
    tled to benefit from the ’072 application’s filing date
    depends on whether the ’072 application provides ade-
    quate written description support for the invention
    claimed in the ’915 patent.
    We affirm the district court’s 2015 decision that Ab-
    bott’s ’915 patent is supported by the written description
    of the ’072 application. As this renders moot Yeda’s
    appeal No. 2015-1663 concerning the district court’s 2008
    decision, we dismiss that appeal for want of jurisdiction.
    BACKGROUND
    A. Patented Technology
    Abbott’s ’915 patent discloses a protein referred to as
    TBP-II. TBP-II binds to and neutralizes a protein called
    Tumor Necrosis Factor α (“TNFα”), which is associated
    with various immunological diseases. The ’915 patent has
    three claims. ’915 patent col. 6 ll. 37−60. Claim 1 is
    representative:
    1. A purified and isolated TNFα-binding protein
    which has a molecular weight of about 42,000 dal-
    tons and has at the N terminus the amino acid se-
    quence
    Xaa Thr Pro Tyr Ala Pro Glu Pro Gly Set
    Thr Cys Arg Leu Arg Glu
    where Xaa is hydrogen, a phenylalanine residue
    (Phe), or the amino acid sequences Ala Phe, Val
    Ala Phe, Gln Val Ala Phe, Ala Gln Val Ala Phe,
    Pro Ala Gln Val Ala Phe or Leu Pro Ala Gln Val
    Ala Phe.
    The U.S. application that resulted in the ’915 patent
    was filed May 4, 1990. It claimed priority to two applica-
    tions for a “novel protein”—the ’072 application, filed May
    9, 1989, and the ’089 application, filed July 5, 1989. J.A.
    5006.
    4         YEDA RESEARCH AND DEVELOPMENT      v. ABBOTT GMBH
    & CO. KG
    The prior art in question is the Engelmann reference,
    which is an article published in January 1990 that de-
    scribes and distinguishes the TBP-I and TBP-II proteins. 1
    The parties do not dispute that Engelmann constitutes
    applicable prior art if the priority date for the ’915 patent
    is May 1990, but not if the ’915 patent benefits from the
    filing date of either the ’072 or the ’089 application. The
    parties do not dispute that the Engelmann reference
    anticipates the ’915 patent if the priority date is May
    1990.
    Neither the ’072 nor the ’089 application discloses the
    full N-terminus sequence claimed in the ’915 patent.
    Instead, they disclose a partial N-terminus sequence, a
    protocol for obtaining the protein from its biological
    source, and additional properties of the protein, such as
    molecular weight, biological activity, and degradation
    characteristics when exposed to trypsin. The parties
    agree that the only protein containing the N-terminus
    sequence set forth in the ’072 application is TBP-II—i.e.,
    the same protein claimed in the ’915 patent. J.A. 5024.
    B. Procedural History
    In 1996, the Board declared Interference No. 103,625
    between Abbott’s ’915 patent and Yeda’s Application No.
    07/930,443. The Board assigned Abbott the May 1990
    filing date of the application that became the ’915 patent
    and held that the ’915 patent was invalid as anticipated
    by Engelmann. Abbott filed suit in federal district court
    seeking review of the Board’s final decision. In 2008, the
    district court granted summary judgment for Abbott,
    holding that the ’089 patent inherently discloses the
    1 Dr. Hartmut Engelmann et al. published “Two
    Tumor Necrosis Factor-Binding Proteins Purified from
    Human Urine” in the Journal of Biological Chemistry on
    January 16, 1990. J.A. 5009.
    YEDA RESEARCH AND DEVELOPMENT V. ABBOTT GMBH             5
    & CO. KG
    TBP-II protein and provides an adequate written descrip-
    tion of the invention claimed in the ’915 application. The
    district court vacated the Board’s decision and remanded
    for further proceedings.
    On remand, the Board reversed course. In 2010, the
    Board held that the ’072 application sufficiently disclosed
    TBP-II for the ’915 patent to benefit from the ’072 appli-
    cation’s May 1989 filing date. Yeda filed a district court
    action seeking review of the Board’s 2010 determination.
    In 2015, the district court affirmed the Board’s decision
    and granted Abbott summary judgment.
    Yeda appeals the district court’s 2008 and 2015 deci-
    sions. We have jurisdiction over these appeals pursuant
    to 28 U.S.C. § 1295(a)(4)(C).
    STANDARD OF REVIEW
    This court reviews de novo a district court’s grant of
    summary judgment in an interference action. Boston Sci.
    Scimed, Inc. v. Medtronic Vascular, Inc., 
    497 F.3d 1293
    ,
    1296 (Fed. Cir. 2007). We review de novo the district
    court’s legal determinations. See Rolls-Royce, PLC v.
    United Techs. Corp., 
    603 F.3d 1325
    , 1330 (Fed. Cir. 2010).
    The Board’s factual findings, including those relied on by
    the district court, are reviewed for substantial evidence.
    In re Gartside, 
    203 F.3d 1305
    , 1311−15 (Fed. Cir. 2000).
    Substantial evidence exists where a reasonable mind
    could accept it as adequate support for a conclusion. 
    Id. at 1312
    (citing Consol. Edison Co. v. NLRB, 
    305 U.S. 197
    ,
    229−30 (1938)).
    DISCUSSION
    Yeda raises three arguments on appeal. First, Yeda
    challenges the legal standard applied by the district court
    to determine whether there was adequate written de-
    scription support for the ’915 patent in the ’072 applica-
    tion. Second, Yeda argues that the prosecution history
    precludes Abbott from relying on inherent disclosure.
    6         YEDA RESEARCH AND DEVELOPMENT    v. ABBOTT GMBH
    & CO. KG
    Third, Yeda asserts that the district court erred in hold-
    ing that the Board’s finding of adequate written descrip-
    tion was supported by substantial evidence.
    We first address the legal standard for written de-
    scription support. In order for the claims of the ’915
    patent to benefit from the ’072 application’s filing date,
    the claimed invention must be disclosed by the ’072
    application. 35 U.S.C. §§ 112, 120; see Kennecott Corp. v.
    Kyocera Int’l, Inc., 
    835 F.2d 1419
    , 1421 (Fed. Cir. 1987).
    The invention must be disclosed in a way that clearly
    allows a person of ordinary skill to recognize that the
    inventor invented what is claimed and possessed the
    claimed subject matter at the date of filing. Ariad Phar-
    maceuticals, Inc. v. Eli Lilly & Co., 
    598 F.3d 1336
    , 1351
    (Fed. Cir. 2010) (en banc).
    Yeda argues that the district court failed to apply the
    correct test for determining the sufficiency of the written
    description. According to Yeda, Abbott must show that at
    the time the ’072 application was filed, a person of ordi-
    nary skill in the art would have understood that the
    partial N-terminus sequence in the ’072 application
    included the additional amino acids identified in the ’915
    patent claims at issue. Abbott responds that the district
    court correctly held that the ’072 application need only
    describe and enable the TBP-II protein, and that a protein
    can be adequately described when a partial amino acid
    sequence is disclosed along with other biological charac-
    teristics.
    Under the doctrine of inherent disclosure, when a
    specification describes an invention that has certain
    undisclosed yet inherent properties, that specification
    serves as adequate written description to support a sub-
    sequent patent application that explicitly recites the
    invention’s inherent properties. See 
    Kennecott, 835 F.2d at 1423
    . In this case, it is undisputed that TBP-II is the
    only protein with the same partial N-terminus sequence
    YEDA RESEARCH AND DEVELOPMENT V. ABBOTT GMBH             7
    & CO. KG
    and additional traits disclosed in the ’072 applica-
    tion. J.A. 5024. Therefore, the ’072 application inherent-
    ly discloses the remaining amino acids in the N-terminus
    sequence of TBP-II and serves as adequate written de-
    scription support for the patent claiming TBP-II. It is not
    necessary for an application to disclose a protein’s com-
    plete N-terminus sequence in order to provide an ade-
    quate written description of that protein. Yeda relies on
    two cases where we declined to find inherent disclosure to
    argue that the doctrine of inherent disclosure does not
    extend to this case: Hyatt v. Boone, 
    146 F.3d 1348
    (Fed.
    Cir. 1998) and In re Wallach, 
    378 F.3d 1330
    (Fed. Cir.
    2004). We disagree. Neither Hyatt nor Wallach involved
    the situation present in this case, where it is undisputed
    that the invention described in an earlier application was
    the exact invention claimed by the later patent.
    Yeda also argues that prosecution history belies Ab-
    bott’s reliance on inherent disclosure. Yeda notes that in
    “the context of priority determinations, the allegedly
    inherent limitation cannot be material to the patentabil-
    ity of the invention.” Yeda asserts that the amino acids
    missing from the ’072 application are material because
    Abbott relied upon their absence to distinguish the prior
    art during prosecution of the ’915 patent. See Hitzeman v.
    Rutter, 
    243 F.3d 1345
    , 1355 (Fed. Cir. 2001). The prose-
    cution history, however, does not support Yeda’s argu-
    ment.
    During prosecution of the ’915 patent, the examiner
    rejected claims based on prior art that disclosed a protein
    with the same source, weight, and function as the protein
    claimed in the ’915 patent. J.A. 9251. Abbott relied on
    the Engelmann article to argue that the cited art con-
    cerned only TBP-I, and that TBP-II includes a sequence of
    five amino acids not present in TBP-I that match the
    chain recited in the ’915 patent claims. J.A. 9268,
    9276−77. Abbott’s response did not solely rely on amino
    acids missing from the priority applications; three of the
    8          YEDA RESEARCH AND DEVELOPMENT      v. ABBOTT GMBH
    & CO. KG
    five amino acids disclosed in Engelmann were disclosed in
    the ’072 application and were themselves sufficient to
    distinguish TBP-I from TBP-II.
    Finally, we reject Yeda’s argument that the district
    court erred in finding that the Board’s conclusion that the
    ’072 application provides written description for the ’915
    patent is supported by substantial evidence. As the
    district court noted, the Board’s decision rested on the
    facts that the ’072 application identified nine of the fifteen
    amino acids of the N-terminus sequences recited in the
    relevant claim, as well as several biological characteristics
    of the protein. J.A. 5028. The parties do not dispute that
    no known protein other than TBP-II matches these char-
    acteristics. The district court correctly found that the
    Board’s decision was supported by substantial evidence.
    CONCLUSION
    Because the ’072 application provides an adequate
    written description of the protein claimed in Abbott’s ’915
    patent, the ’915 patent benefits from the priority date of
    the ’072 application. We affirm the district court’s 2015
    decision. We dismiss Yeda’s appeal No. 2015-1663 from
    the district court’s 2008 decision for lack of jurisdiction, as
    it is now moot.
    AFFIRMED
    COSTS
    No costs.